Harnessing Ion-Binding Sites for GPCR Pharmacology.

ABSTRACT: Endogenous ions play important roles in the function and pharmacology of G-protein coupled receptors (GPCRs). Historically the evidence for ionic modulation of GPCR function dates to 1973 with studies of opioid receptors, where it was demonstrated that physiologic concentrations of sodium allosterically attenuated agonist binding. This Na⁺-selective effect was distinct from effects of other monovalent and divalent cations, with the latter usually counteracting sodium's negative allosteric modulation of binding. Since then, numerous studies documenting the effects of mono- and divalent ions on GPCR function have been published. While ions can act selectively and nonselectively at many sites in different receptors, the discovery of the conserved sodium ion site in class A GPCR str

SUBMITTER: Zarzycka B 

PROVIDER: S-EPMC6782022 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature